Примери за използване на All treatment groups на Английски и техните преводи на Български
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Medicine
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Colloquial
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Ecclesiastic
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Ecclesiastic
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Cure rates were 90- 93% across all treatment groups.
All treatment groups had a reduction in HbA1c compared to baseline.
Increased mortality was noted in all treatment groups.
All treatment groups had a significant reduction in HbA1c compared to baseline.
The cure rates were 99% to 100% across all treatment groups.
The dose of corticosteroids used in all treatment groups was tapered during the first 6 months following transplantation.
Most patients were non-naive to chemotherapy(78.5%) across all treatment groups.
The majority of patients in all treatment groups were Caucasian(90%).
SSRIs, SNRIs SSRIs andSNRIs increased the risk of bleeding in RE-LY in all treatment groups.
At screening, the mean age was similar in all treatment groups in both studies, ranging between 61.5 and 65.3 years.
In Study 735, lung function, symptom control, andreliever use were similar in all treatment groups.
Patients in all treatment groups with an inadequate response at week 16 received rescue therapy(modification to background therapy).
In the ovary, there was an increase in sex-cord stromal tumours, tubulostromal tumours, granulosa cell tumours andluteomas in all treatment groups.
The most frequent AEs experienced by patients in all treatment groups were hypotension(48.7%), nausea(31.9%), vomiting(22.1%) and cramps.
In all treatment groups, including placebo, improvements in PAC-SYM domains observed in Kodiac 4 were maintained for patients continuing in Kodiac 7.
Histological assessment of bone biopsies from all treatment groups revealed formation of normal lamellar bone in all treated subjects.
Across all treatment groups, the mean baseline PASI score was 19.7 and the baseline PGA score ranged from“mild”(< 1%) to“moderate”(48%) to“severe”(46%) to“very severe”(6%).
The rates of events in the composite endpoint were low across all treatment groups and were similar or lower for each of the active treatments compared to placebo.
Across all treatment groups, the mean baseline PASI score was 19.7 and the baseline PGA score ranged from“ mild”(< 1%) to“ moderate”(48%) to“ severe”(46%) to“ very severe”(6%).
In patients with moderate renal impairment,the incidence of renalrelated adverse reactions was similar across all treatment groups: Zurampic 200 mg(12.7%), Zurampic 400 mg(16.3%) and placebo(13.3%).
Across all treatment groups, the mean baseline PASI score was 18.9 and the baseline PGA score ranged from“moderate”(53% of subjects included) to“severe”(41%) to“very severe”(6%).
The following table shows the incidence of MACE andHazard Ratios vs placebo for all treatment groups during treatment, and cumulative for treatment plus 30 days and through end of study.
Across all treatment groups, the mean baseline PASI score was 19.7 and the baseline PGA score ranged from“mild”(< 1%) to“moderate”(48%) to“severe”(46%) to“very severe”(6%).
Statistically significant increases from treatment baseline in absolute FVC volume were seen at most visits for all treatment groups combined and for each of the prior TKT024 treatment groups. .
In the concomitant TCS study(CHRONOS), across all treatment groups, the mean age was 37.1, the mean weight was 74.5 kg, 39.7% were female, 66.2% were white, 27.2% were Asian, and 4.6% were black.
There was an overall increased frequency of adverse events in the older population compared to patients<65 years which was comparable across all treatment groups, including placebo.
SSRIs, SNRIs SSRIs andSNRIs increased the risk of bleeding in all treatment groups of a phase III clinical trial comparing dabigatran to warfarin for stroke prevention in atrial fibrillation patients(RE-LY).
Changes in urinary GAG levels were the earliest signs of clinical improvement with idursulfase treatment andthe greatest decreases in urinary GAG were seen within the first 4 months of treatment in all treatment groups;
Across all treatment groups, the mean baseline PASI score was 18.9 and the baseline Physician' s Global Assessment(PGA) score ranged from“ moderate”(53% of subjects included) to“ severe”(41%) to“ very severe”(6%).
The frequency of grade 4(life-threatening) and grade 5(fatal)infections was low in all treatment groups, but in PPMS it was higher with Ocrevus compared with placebo for life-threatening(1.6% vs 0.4%) and fatal(0.6% vs 0%) infections.